Job Title: Integral Development Associate Medical Director
Introduction to role:
This role is based in Warsaw, with an on-site commitment of three days a week. Fluency in English is required.
Are you ready to put your medical oncology training to work at the heart of hemato-oncology development, where every decision you make strengthens patient safety and accelerates innovative trials? Do you thrive at the intersection of patient safety, trial strategy, and cross-functional leadership? In this role, you will be a key medical voice guiding global studies from early design through closeout, ensuring robust risk-benefit oversight and scientific rigor.
You will partner closely with Clinical Operations and cross-functional experts to shape protocols, engage investigators and external experts, and translate emerging data into decisive actions that keep studies on track and patients safe. You will also have the opportunity to lead process improvements and contribute to cross-asset,



cross-indication initiatives—broadening your impact as our oncology portfolio advances across multiple indications and stages. Your work will directly influence how we identify patients earlier, execute trials faster, and bring transformative therapies to those who need them most.
Accountabilities:
Responsible for ensuring the risk-benefit of a clinical study, maintaining the highest ethical and safety standards in compliance with FDA, EMEA, ICH, and GCP guidelines as well as AZ SOPs regarding safety.
Work cross-functionally in the design and implementation of clinical hemato-oncology projects as a member of the Clinical Sub-Team (CST), ensuring scientific and clinical rigor.
Contribute to the development of program strategy for assigned compounds/programs and collaborate with team members to develop compelling business cases for governance approval.
Provide clinical input to influence study design through collaboration with primary investigators, key external experts (KEE), study sites, team memb

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